| Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes TJ Edwards, EH Sherr, AJ Barkovich, LJ Richards Brain 137 (6), 1579-1613, 2014 | 358 | 2014 |
| Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance APL Marsh, D Heron, TJ Edwards, A Quartier, C Galea, C Nava, ... Nature genetics 49 (4), 511-514, 2017 | 97 | 2017 |
| DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome APL Marsh, TJ Edwards, C Galea, HM Cooper, EC Engle, SS Jamuar, ... Human mutation 39 (1), 23-39, 2018 | 64 | 2018 |
| Altered structural connectome in adolescent socially isolated mice C Liu, Y Li, TJ Edwards, ND Kurniawan, LJ Richards, T Jiang Neuroimage 139, 259-270, 2016 | 53 | 2016 |
| NFIB haploinsufficiency is associated with intellectual disability and macrocephaly I Schanze, J Bunt, JWC Lim, D Schanze, RJ Dean, M Alders, P Blanchet, ... The American Journal of Human Genetics 103 (5), 752-768, 2018 | 41 | 2018 |
| Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice GL Galea, E Maniou, TJ Edwards, AR Marshall, I Ampartzidis, ... Nature communications 12 (1), 1159, 2021 | 28 | 2021 |
| EMX1 regulates NRP1-mediated wiring of the mouse anterior cingulate cortex JWC Lim, ALS Donahoo, J Bunt, TJ Edwards, LR Fenlon, Y Liu, J Zhou, ... Development 142 (21), 3746-3757, 2015 | 19 | 2015 |
| Altered structural connectivity networks in a mouse model of complete and partial dysgenesis of the corpus callosum TJ Edwards, LR Fenlon, RJ Dean, J Bunt, EH Sherr, LJ Richards, ... NeuroImage 217, 116868, 2020 | 17 | 2020 |
| Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutations M Spencer‐Smith, JL Knight, E Lacaze, Irc5 Consortium, C Depienne, ... Developmental Medicine & Child Neurology 62 (6), 758-762, 2020 | 17 | 2020 |
| Astroglial-mediated remodeling of the interhemispheric midline during telencephalic development is exclusive to eutherian mammals I Gobius, R Suárez, L Morcom, A Paolino, TJ Edwards, P Kozulin, ... Neural Development 12, 1-7, 2017 | 13 | 2017 |
| DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation L Morcom, TJ Edwards, E Rider, D Jones-Davis, JWC Lim, KS Chen, ... Elife 10, e61618, 2021 | 11 | 2021 |
| Cortical architecture, midline guidance, and tractography of 3D white matter tracts LR Morcom, TJ Edwards, LJ Richards Axons and brain architecture, 289-313, 2016 | 10 | 2016 |
| DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation L Morcom, I Gobius, APL Marsh, R Suárez, JWC Lim, C Bridges, Y Ye, ... Elife 10, e61769, 2021 | 7 | 2021 |
| Chapter 14-Cortical architecture, midline guidance, and tractography of 3D white matter tracts LR Morcom, TJ Edwards, LJ Richards Axons and Brain Architecture, 289-313, 2016 | 5 | 2016 |
| Reply: ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability TJ Edwards, EH Sherr, AJ Barkovich, LJ Richards Brain, 2016 | 4 | 2016 |
| Mirror movements and callosal dysgenesis in a family with a DCC mutation: Neuropsychological and neuroimaging outcomes JL Knight, MS Barker, TJ Edwards, JM Barnby, LJ Richards, GA Robinson Cortex 161, 38-50, 2023 | 3 | 2023 |
| Teaching NeuroImages: Imaging features of DCC-mediated mirror movements and isolated agenesis of the corpus callosum TJ Edwards, APL Marsh, PJ Lockhart, LJ Richards, RJ Leventer Neurology 91 (9), e886-e887, 2018 | 3 | 2018 |
| The DCC receptor regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation L Morcom, I Gobius, APL Marsh, R Suárez, C Bridges, Y Ye, LR Fenlon, ... bioRxiv, 2020.08. 03.233593, 2020 | | 2020 |
| Genetics and structural connectivity in agenesis of the corpus callosum T Edwards | | 2019 |
| Dominant mutations in DCC cause isolated agenesis of the corpus callosum with sex specific penetrance APL Marsh, D Heron, TJ Edwards, A Quartier, A Rastetter, C Nava, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 110-111, 2018 | | 2018 |
Linda J. RichardsBrain Development and Disorders Laboratory, Washington University in St Louis_NeuroscienceVerified email at wustl.edu